A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161470



Internal ID7906184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1900722..2632569hg38UCSC Ensembl
Innerchr3:1942406..2674253hg19UCSC Ensembl
Innerchr3:1917406..2649253hg18UCSC Ensembl
Innerchr3:1917406..2649253hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38731848
hg19731848
hg18731848
hg17731848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422409
Supporting Variants
SamplesND05461
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161470
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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